Fraxa

Human FMR1 wild-type allele is located in the vicinity of Xq27.3 and is approximately 39 kb in length. This allele, which encodes fragile X mental retardation protein 1, may play a role in the mediation of mRNA transport. Amplification of a trinucleotide repeat (CGG) within the gene is associated with fragile X syndrome.

Disease Alternative Name

fmrp

premature ovarian failure 1 gene

fragile x mental retardation 1 wt allele

fmr1 wt allele

mgc87458

pof

MainRecentTopDoctors

Recent Cases of Fraxa

Browse recently discussed Fraxa cases by specialists

Dr. Manisha Kanade

General Practice (Homeopathy)

35 yr old female c/o heavy menstrual bleeding 7-8days with regular periods . Usg shows mild bulky uterus anteverted with fibroid 22.0× 21.0× 15.0mm endometrial polyp. Homoeopathic treatment given- fraxiunus americana Q , hertone syp , silic...See More

23 Views

, 3 Likes

, 11 Answers

LikeAnswers Share

11 Answers3 Likes